Herpes simplex virus: receptors and ligands for cell entry

被引:437
作者
Spear, PG [1 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
关键词
D O I
10.1111/j.1462-5822.2004.00389.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Entry of herpes simplex virus (HSV) into cells depends upon multiple cell surface receptors and multiple proteins on the surface of the virion. The cell surface receptors include heparan sulphate chains on cell surface proteoglycans, a member of the tumor necrosis factor (TNF) receptor family and two members of the immunoglobulin superfamily related to the poliovirus receptor. The HSV ligands for these receptors are the envelope glycoproteins gB and gC for heparan sulphate and gD for the protein receptors and specific sites in heparan sulphate generated by certain 3-O-sulfotransferases. HSV gC also binds to the C3b component of complement and can block complement-mediated neutralization of virus. The purposes of this review are to summarize available information about these cell surface receptors and the viral ligands, gC and gD, and to discuss roles of these viral glycoproteins in immune evasion and cellular responses as well as in viral entry.
引用
收藏
页码:401 / 410
页数:10
相关论文
共 77 条
[21]   Transcription from the gene encoding the herpesvirus entry receptor nectin-1 (HveC) in nervous tissue of adult mouse [J].
Haarr, L ;
Shukla, D ;
Rodahl, E ;
Dal Canto, MC ;
Spear, PG .
VIROLOGY, 2001, 287 (02) :301-309
[22]   GLYCOPROTEIN-C-INDEPENDENT BINDING OF HERPES-SIMPLEX VIRUS TO CELLS REQUIRES CELL-SURFACE HEPARAN-SULFATE AND GLYCOPROTEIN-B [J].
HEROLD, BC ;
VISALLI, RJ ;
SUSMARSKI, N ;
BRANDT, CR ;
SPEAR, PG .
JOURNAL OF GENERAL VIROLOGY, 1994, 75 :1211-1222
[23]   GLYCOPROTEIN-C OF HERPES-SIMPLEX VIRUS TYPE-1 PLAYS A PRINCIPAL ROLE IN THE ADSORPTION OF VIRUS TO CELLS AND IN INFECTIVITY [J].
HEROLD, BC ;
WUDUNN, D ;
SOLTYS, N ;
SPEAR, PG .
JOURNAL OF VIROLOGY, 1991, 65 (03) :1090-1098
[24]   GLYCOPROTEIN-C OF HERPES-SIMPLEX VIRUS TYPE-1 IS ESSENTIAL FOR THE VIRUS TO EVADE ANTIBODY-INDEPENDENT COMPLEMENT-MEDIATED VIRUS INACTIVATION AND LYSIS OF VIRUS-INFECTED CELLS [J].
HIDAKA, Y ;
SAKAI, Y ;
TOH, Y ;
MORI, R .
JOURNAL OF GENERAL VIROLOGY, 1991, 72 :915-921
[25]   ATAR, a novel tumor necrosis factor receptor family member, signals through TRAF2 and TRAF5 [J].
Hsu, HL ;
Solovyev, I ;
Colombero, A ;
Elliott, R ;
Kelley, M ;
Boyle, WJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (21) :13471-13474
[26]   SPECIES SELECTIVE INTERACTION OF ALPHAHERPESVIRINAE WITH THE UNSPECIFIC IMMUNE-SYSTEM OF THE HOST [J].
HUEMER, HP ;
LARCHER, C ;
LITTELVANDENHURK, SV ;
BABIUK, LA .
ARCHIVES OF VIROLOGY, 1993, 130 (3-4) :353-364
[27]   STRUCTURAL BASIS OF C3B BINDING BY GLYCOPROTEIN-C OF HERPES-SIMPLEX VIRUS [J].
HUNG, SL ;
SRINIVASAN, S ;
FRIEDMAN, HM ;
EISENBERG, RJ ;
COHEN, GH .
JOURNAL OF VIROLOGY, 1992, 66 (07) :4013-4027
[28]   THE INTERACTION OF GLYCOPROTEIN-C OF HERPES-SIMPLEX VIRUS TYPE-1 AND TYPE-2 WITH THE ALTERNATIVE COMPLEMENT PATHWAY [J].
HUNG, SL ;
PENG, C ;
KOSTAVASILI, I ;
FRIEDMAN, HM ;
LAMBRIS, JD ;
EISENBERG, RJ ;
COHEN, GH .
VIROLOGY, 1994, 203 (02) :299-312
[29]   Effects of linker-insertion mutations in herpes simplex virus 1 gD on glycoprotein-induced fusion with cells expressing HVEM or nectin-1 [J].
Jogger, CR ;
Montgomery, RI ;
Spear, PG .
VIROLOGY, 2004, 318 (01) :318-326
[30]   Herpes simplex virus gE/gI sorts nascent virions to epithelial cell junctions, promoting virus spread [J].
Johnson, DC ;
Webb, M ;
Wisner, TW ;
Brunetti, C .
JOURNAL OF VIROLOGY, 2001, 75 (02) :821-833